ClinicalTrials.gg
CompletedNCT00006734Updated Aug 3, 2023

Comparison of Combination Chemotherapy Regimens in Treating Patients With Ewing's Sarcoma or Neuroectodermal Tumor

A Phase 3 interventional study of filgrastim and cyclophosphamide in Sarcoma, sponsored by Children's Oncology Group. Completed at 239 sites in 7 countries. Open to participants aged 0 Years to 50 Years. Per ClinicalTrials.gov, last updated 2023-08-03.

Sponsored by Children's Oncology Group · Phase 3, Interventional, and Treatment

Phase
Phase 3
Study type
Interventional
Enrollment
587
Allocation
Randomized
Ages
0 Years to 50 Years
Sex
All
01

Study summary

RATIONALE: Drugs used in chemotherapy work in different ways to stop tumor cells from dividing so they stop growing or die. Radiation therapy uses high-energy x-rays to damage tumor cells. It is not yet known which chemotherapy regimen combined with radiation therapy and/or surgery is more effective in treating Ewing's sarcoma or primitive neuroectodermal tumor.

PURPOSE: Randomized phase III trial to compare the effectiveness of different chemotherapy regimens combined with radiation therapy and/or surgery in treating patients who have Ewing's sarcoma or primitive neuroectodermal tumor.

Read the detailed description

OBJECTIVES:

  • Compare the effect of interval-compressed vs standard chemotherapy in terms of event-free survival and overall survival in patients with newly diagnosed, localized Ewing's sarcoma or peripheral primitive neuroectodermal tumor.

OUTLINE: This is a randomized, multicenter study. Patients are stratified according to age (under 18 years vs 18 years and over) and location of primary disease (pelvic vs nonpelvic). Patients are randomized to 1 of 2 treatment arms for induction and continuation therapy.

  • Induction therapy (weeks 1-12):

    • Arm I: Patients receive alternating courses of chemotherapy consisting of vincristine IV on day 1, doxorubicin IV continuously over 48 hours on days 1 and 2, and cyclophosphamide IV over 1 hour on day 1 for courses 1 and 3 and ifosfamide IV over 1 hour and etoposide IV over 1-2 hours on days 1-5 for courses 2 and 4. Beginning 24 hours after the last dose of chemotherapy for each course, patients receive filgrastim (G-CSF) subcutaneously (SC) daily until blood counts recover. Treatment continues every 3 weeks for 4 courses.
    • Arm II: Patients receive alternating courses of chemotherapy consisting of vincristine, doxorubicin, and cyclophosphamide as in arm I for courses 1, 3, and 5 and ifosfamide and etoposide as in arm I for courses 2, 4, and 6. Patients also receive G-CSF as in arm I. Treatment continues every 2 weeks for 6 courses.

After completion of induction therapy, patients in both arms receive local control treatment to the primary tumor. Patients receive continuation chemotherapy after surgery or concurrently with radiotherapy.

  • Continuation therapy:

    • Arm I (weeks 13-42): Patients receive additional alternating courses of chemotherapy as in arm I of induction therapy with the exception of vincristine and cyclophosphamide alone for courses 7 and/or 11 and/or 13. Patients also receive G-CSF as in induction therapy. Treatment continues every 3 weeks for 10 courses.
    • Arm II (weeks 13-29): Patients receive additional alternating courses of chemotherapy as in arm II of induction therapy with the exception of vincristine and cyclophosphamide alone for courses 9 and/or 11 and/or 13. Patients also receive G-CSF as in induction therapy. Treatment continues every 2 weeks for 8 courses.

Patients are followed every 3 months for 4 years and then every 6 months for 1 year.

PROJECTED ACCRUAL: Approximately 528 patients will be accrued for this study within 4-5 years.

02

Conditions studied

  • Sarcoma

Keywords

  • localized Ewing sarcoma/peripheral primitive neuroectodermal tumor
03

In context

Sarcoma

1,607 studies on the registry are indexed under Sarcoma; 366 are open to participants now.

This study's enrollment of 587 is above the median of 40 across 1,255 interventional studies indexed under Sarcoma.

Browse Sarcoma studies →

Lead sponsor

Children's Oncology Group is the lead sponsor of 448 studies on the registry; 36 are open to participants now.

Of its 12 completed or terminated interventional studies of FDA-regulated products, 11 (92%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
0 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

DISEASE CHARACTERISTICS:

  • confirmed localized Ewing's sarcoma or peripheral primitive neuroectodermal tumor (PNET) of the bone or soft tissues

    • Diagnostic of primary tumor within 30 days of study
  • Paraspinal or bony skull tumors of extradural origin allowed

    • No intradural soft tissue tumors
  • Askin's tumor of the chest wall allowed

    • Chest wall tumors with ipsilateral pleural effusions or ipsilateral pleural-based secondary tumor nodules allowed
    • No contralateral pleural effusions
  • No disease or distant node involvement

    • One pulmonary or pleural nodule greater than 1 cm in diameter OR more than 1 nodule greater than 0.5 cm in diameter are considered pulmonary metastasis
    • Solitary lung nodules of 0.5-1 cm OR multiple nodules of 0.3-0.5 cm allowed unless biopsy positive for tumor
  • Light microscopic appearance (hematoxylin and eosin stained) consistent with Ewing's sarcoma or peripheral PNET
  • No immunohistochemical or ultrastructural evidence of rhabdomyosarcoma
  • No esthesioneuroblastoma
  • Clinically or pathologically involved regional lymph nodes allowed
  • No CNS involvement

PATIENT CHARACTERISTICS:

Age:

  • 50 and under at diagnosis

Performance status:

  • Not specified

:

  • Not specified

Hematopoietic:

  • Not specified

Hepatic:

  • no greater than 1.5 mg/dL

Renal:

  • Creatinine normal for age
  • or isotope at least 75 mL/min

Cardiovascular:

  • Shortening fraction at least 28% by echocardiography OR
  • at least 55% by radionuclide angiogram

Other:

  • Not pregnant or nursing
  • Fertile patients must use effective
  • No other prior except skin cancer diagnosed at least 5 years ago and currently in remission

PRIOR CONCURRENT THERAPY:

Biologic therapy:

  • No prior immunotherapy for skin cancer
  • No concurrent sargramostim (GM-CSF)
  • No concurrent pegfilgrastim

Chemotherapy:

  • No prior chemotherapy

Endocrine therapy:

  • Not specified

Radiotherapy:

  • No prior radiotherapy

Surgery:

  • Prior complete or partial excision of primary tumor allowed
Terms in these criteria, in plain language(10)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Histologically or cytologically confirmed

The diagnosis was confirmed by looking at a sample under a microscope: tissue from a biopsy or surgery (histology), or cells from a fluid or needle sample (cytology).

Your pathology report is the document that shows this.

Biopsy and archival tissue

A biopsy takes a small piece of tissue to examine. “Archival tissue” is a sample already taken, for example at diagnosis, and kept by the hospital.

Whether a stored sample will do depends on when it was taken, how much there is and what the study needs. Ask whether the study accepts your stored sample or needs a new biopsy.

Metastases

Cancer that has spread from where it began to other parts of the body. “Metastatic” cancer is cancer that has spread this way.

Life expectancy

The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.

Bilirubin

A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.

Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.

Creatinine clearance (CrCl)

How quickly the kidneys clear creatinine, a waste product, from the blood. A study may estimate it from a blood test with age, weight and sex (often by the Cockcroft–Gault formula), or measure it using blood and urine collected over a set time. Given in mL/min; higher is better.

GFR and eGFR (kidney filtering)

GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².

Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.

LVEF (left ventricular ejection fraction)

The share of blood the heart’s main pumping chamber (the left ventricle) pushes out with each beat, measured by an echocardiogram (heart ultrasound) or a MUGA scan. About 50–70% is normal.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
587 participants (actual)

Study arms

  • Experimental
    Regimen A

    Test the hypothesis that chemotherapy given every two weeks (Regimen B) will produce higher event-free survival. Treatment will occur in two phases: Induction and Continuation, with 14 cycles of chemotherapy in all. Induction consists of the first twelve weeks (four cycles on Regimen A. The cycles alternate between vincristine sulfate, doxorubicin hydrochloride, cyclophosphamide, MESNA and ifosfamide, etoposide, MESNA. G-CSF (Filgrastim) is given between chemotherapy doses. Local control (Surgery, Radiation Therapy, or a combination) will begin on Week 13 which will be after four cycles of chemotherapy.

    Biological: filgrastim · Drug: cyclophosphamide · Drug: doxorubicin hydrochloride · Drug: etoposide · Drug: ifosfamide · Drug: vincristine sulfate · Procedure: adjuvant therapy · Procedure: conventional surgery · Procedure: neoadjuvant therapy · Radiation: brachytherapy · Radiation: radiation therapy

  • Experimental
    Regimen B

    Conventional every-three-week chemotherapy for patients with Ewing sarcoma and related tumors. Treatment will occur in two phases: Induction and Continuation, with 14 cycles of chemotherapy in all. Induction consists of the first twelve weeks six cycles on Regimen B). The cycles alternate between vincristine sulfate, doxorubicin hydrochloride, cyclophosphamide, MESNA and ifosfamide etoposide MESNA. G-CSF (Filgrastim) is given between chemotherapy doses. Local control (surgery, Radiation Therapy, or a combination) will begin on Week 13, which will be after six cycles of chemotherapy.

    Biological: filgrastim · Drug: cyclophosphamide · Drug: doxorubicin hydrochloride · Drug: etoposide · Drug: ifosfamide · Drug: vincristine sulfate · Procedure: adjuvant therapy · Procedure: conventional surgery · Procedure: neoadjuvant therapy · Radiation: brachytherapy · Radiation: radiation therapy

Interventions

  • Biologicalfilgrastim

    Given IV

    Also known as: GRANULOCYTE COLONY-STIMULATING FACTOR, r-metHuG-CSF, G-CSF, Neupogen, NSC 614629

  • Given IV

    Also known as: CTX, Cytoxan, NSC #026271

  • Given IV

    Also known as: Adriamycin, NSC #123127, IND #7038

  • Given IV

    Also known as: VP-16, VePesid, Etopophos, NSC #141540

  • Given IV

    Also known as: Ifex, NSC #109724

  • Given IV

    Also known as: Oncovin, NSC #067574

  • Procedureadjuvant therapy
  • Procedureconventional surgery
  • Procedureneoadjuvant therapy
  • Radiationbrachytherapy
  • Radiationradiation therapy
06

What researchers measure

Primary outcomes

  1. Event-free survival

    Assessed using a two sided log rank test of 0.05.

    Time frame: Time from study entry until disease progression, death without progression of disease, occurrence of a second malignant neoplasm or last follow-up, whichever comes first, assessed up to 5 years

07

Study locations

239 sites
  • Comprehensive Cancer Center at University of Alabama at Birmingham
    Birmingham, Alabama 35233, United States
  • University of South Alabama Cancer Research Institute
    Mobile, Alabama 36604, United States
  • Phoenix Children's Hospital
    Phoenix, Arizona 85016, United States
  • Arizona Cancer Center at University of Arizona Health Sciences Center
    Tucson, Arizona 85724, United States
  • Arkansas Cancer Research Center at University of Arkansas for Medical Sciences
    Little Rock, Arkansas 72205, United States
  • Southern California Permanente Medical Group
    Downey, California 90242, United States
  • City of Hope Comprehensive Cancer Center
    Duarte, California 91010-3000, United States
  • Rebecca and John Moores UCSD Cancer Center
    La Jolla, California 92093-0658, United States
  • Loma Linda University Cancer Institute at Loma Linda University Medical Center
    Loma Linda, California 92354, United States
  • Jonathan Jaques Children's Cancer Center at Miller Children's Hospital
    Long Beach, California 90801-1428, United States
  • Children's Hospital Los Angeles
    Los Angeles, California 90027-0700, United States
  • Samuel Oschin Comprehensive Cancer Institute at Cedars-Sinai Medical Center
    Los Angeles, California 90048, United States
  • Jonsson Comprehensive Cancer Center at UCLA
    Los Angeles, California 90095-1781, United States
  • Children's Hospital Central California
    Madera, California 93638-8762, United States
  • Children's Hospital and Research Center at Oakland
    Oakland, California 94609-1809, United States
  • Chao Family Comprehensive Cancer Center at University of California Irvine Medical Center
    Orange, California 92868, United States
  • Children's Hospital of Orange County
    Orange, California 92868, United States
  • Lucile Packard Children's Hospital at Stanford University Medical Center
    Palo Alto, California 94304, United States
  • Sutter Cancer Center
    Sacramento, California 95816, United States
  • University of California Davis Cancer Center
    Sacramento, California 95817, United States
  • Kaiser Permanente Medical Center - Sacramento
    Sacramento, California 95825, United States
  • Kaiser Permanente Medical Center/Kaiser Foundation Hospital - San Diego
    San Diego, California 92120, United States
  • Children's Hospital and Health Center - San Diego
    San Diego, California 92123-4282, United States
  • UCSF Comprehensive Cancer Center
    San Francisco, California 94143, United States
  • Santa Barbara Cottage Hospital
    Santa Barbara, California 93102, United States
  • Kaiser Permanente Medical Center - Santa Clara
    Santa Clara, California 95051-5386, United States
  • General Robert Huyser Cancer Center at David Grant Medical Center
    Travis Air Force Base, California 94535, United States
  • Children's Hospital Cancer Center
    Denver, Colorado 80218, United States
  • Presbyterian - St. Luke's Medical Center
    Denver, Colorado 80218, United States
  • Carole and Ray Neag Comprehensive Cancer Center at the University of Connecticut Health Center
    Farmington, Connecticut 06360-7106, United States
  • Yale Comprehensive Cancer Center
    New Haven, Connecticut 06520-8064, United States
  • Alfred I. duPont Hospital for Children
    Wilmington, Delaware 19899, United States
  • Lombardi Cancer Center at Georgetown University Medical Center
    Washington, District of Columbia 20007, United States
  • Children's National Medical Center
    Washington, District of Columbia 20010-2970, United States
  • Broward General Medical Center
    Fort Lauderdale, Florida 33316, United States
  • Children's Hospital of Southwest Florida
    Fort Myers, Florida 33908, United States
  • University of Florida Shands Cancer Center
    Gainesville, Florida 32610-0296, United States
  • Joe DiMaggio Children's Hospital at Memorial
    Hollywood, Florida 33021, United States
  • Nemours Children's Clinic
    Jacksonville, Florida 32207, United States
  • Jackson Memorial Hospital
    Miami, Florida 33136, United States
  • Miami Children's Hospital
    Miami, Florida 33155, United States
  • Baptist-South Miami Regional Cancer Program
    Miami, Florida 33176-2197, United States
  • Florida Hospital Cancer Institute
    Orlando, Florida 32804, United States
  • Nemours Children's Clinic-Orlando
    Orlando, Florida 32806, United States
  • Sacred Heart Children's Hospital
    Pensacola, Florida 32504, United States
  • All Children's Hospital
    Saint Petersburg, Florida 33701, United States
  • St. Joseph's Children's Hospital of Tampa
    Tampa, Florida 33677-4227, United States
  • Kaplan Cancer Center at St. Mary's Medical Center
    West Palm Beach, Florida 33407, United States
  • AFLAC Cancer Center and Blood Disorders Service of Children's Healthcare of Atlanta - Scottish Rite Campus
    Atlanta, Georgia 30342, United States
  • MBCCOP-Medical College of Georgia Cancer Center
    Augusta, Georgia 30912-4000, United States
  • Medical Center of Central Georgia
    Macon, Georgia 31201, United States
  • Curtis & Elizabeth Anderson Cancer Institute at Memorial Health University Medical Center
    Savannah, Georgia 31405, United States
  • Cancer Research Center of Hawaii
    Honolulu, Hawaii 96813, United States
  • Tripler Army Medical Center
    Honolulu, Hawaii 96859-5000, United States
  • St. Luke's Mountain States Tumor Institute - Boise
    Boise, Idaho 83712, United States
  • University of Chicago Cancer Research Center
    Chicago, Illinois 60601, United States
  • Rush University Medical Center
    Chicago, Illinois 60612, United States
  • University of Illinois Medical Center
    Chicago, Illinois 60612, United States
  • Children's Memorial Hospital - Chicago
    Chicago, Illinois 60614, United States
  • Advocate Hope Children's Hospital
    Oak Lawn, Illinois 60453, United States
  • Lutheran General Cancer Care Center
    Park Ridge, Illinois 60068-1174, United States
  • Saint Jude Midwest Affiliate
    Peoria, Illinois 61637, United States
  • Southern Illinois University School of Medicine
    Springfield, Illinois 62794-9658, United States
  • Riley Children Cancer Center at Riley Hospital for Children
    Indianapolis, Indiana 46202-5225, United States
  • St. Vincent Hospitals and Health Care Centers
    Indianapolis, Indiana 46260, United States
  • Blank Children's Hospital
    Des Moines, Iowa 50308, United States
  • Holden Comprehensive Cancer Center at University of Iowa
    Iowa City, Iowa 52242-1009, United States
  • Wesley Medical Center
    Wichita, Kansas 67214, United States
  • Markey Cancer Center at University of Kentucky Chandler Medical Center
    Lexington, Kentucky 40536-0284, United States
  • Kosair Children's Hospital
    Louisville, Kentucky 40202-3830, United States
  • MBCCOP - LSU Health Sciences Center
    New Orleans, Louisiana 70112, United States
  • Tulane Cancer Center at Tulane University Hospital and Clinic
    New Orleans, Louisiana 70112, United States
  • Children's Hospital of New Orleans
    New Orleans, Louisiana 70118, United States
  • Ochsner Cancer Institute at Ochsner Clinic Foundation
    New Orleans, Louisiana 70121, United States
  • Pediatric Specialty Clinic at Eastern Maine Medical Center
    Bangor, Maine 04401, United States
  • Maine Children's Cancer Program
    Scarborough, Maine 04074-9308, United States
  • Greenebaum Cancer Center at University of Maryland Medical Center
    Baltimore, Maryland 21201-1595, United States
  • Alvin and Lois Lapidus Cancer Institute at Sinai Hospital
    Baltimore, Maryland 21215, United States
  • Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
    Baltimore, Maryland 21231-7223, United States
  • Walter Reed Army Medical Center
    Silver Spring, Maryland 20910, United States
  • Floating Hospital for Children
    Boston, Massachusetts 02111, United States
  • Dana-Farber/Harvard Cancer Center at Dana Farber Cancer Institute
    Boston, Massachusetts 02115, United States
  • Baystate Regional Cancer Program at D'Amour Center for Cancer Care
    Springfield, Massachusetts 01107, United States
  • UMASS Memorial Cancer Center - University Campus
    Worcester, Massachusetts 01655, United States
  • University of Michigan Comprehensive Cancer Center
    Ann Arbor, Michigan 48109-0914, United States
  • Children's Hospital of Michigan
    Detroit, Michigan 48201, United States
  • Van Elslander Cancer Center at St. John Hospital and Medical Center
    Detroit, Michigan 48236, United States
  • Hurley Medical Center
    Flint, Michigan 48503, United States
  • DeVos Children's Hospital
    Grand Rapids, Michigan 49503, United States
  • Bronson Methodist Hospital
    Kalamazoo, Michigan 49007-5364, United States
  • Breslin Cancer Center at Ingham Regional Medical Center
    Lansing, Michigan 48910, United States
  • William Beaumont Hospital - Royal Oak Campus
    Royal Oak, Michigan 48073-6769, United States
  • St. Mary's - Duluth Clinic Cancer Center
    Duluth, Minnesota 55805, United States
  • Children's Hospitals and Clinics - Minneapolis/St. Paul
    Minneapolis, Minnesota 55404, United States
  • Mayo Clinic Cancer Center
    Rochester, Minnesota 55905, United States
  • University of Mississippi Medical Center
    Jackson, Mississippi 39216-4505, United States
  • Children's Mercy Hospital
    Kansas City, Missouri 64108, United States
  • Cardinal Glennon Children's Hospital
    Saint Louis, Missouri 63104, United States
  • St. Louis Children's Hospital
    Saint Louis, Missouri 63110, United States
  • CCOP - Montana Cancer Consortium
    Billings, Montana 59101, United States

Showing the first 100 of 239 sites across 7 countries. Choose a country and city above to see the rest.

08

References and documents

Publications

  • van Doorninck JA, Ji L, Schaub B, Shimada H, Wing MR, Krailo MD, Lessnick SL, Marina N, Triche TJ, Sposto R, Womer RB, Lawlor ER. Current treatment protocols have eliminated the prognostic advantage of type 1 fusions in Ewing sarcoma: a report from the Children's Oncology Group. J Clin Oncol. 2010 Apr 20;28(12):1989-94. doi: 10.1200/JCO.2009.24.5845. Epub 2010 Mar 22. PubMed 20308669 ↗
  • Womer RB, West DC, Krailo MD, Dickman PS, Pawel BR, Grier HE, Marcus K, Sailer S, Healey JH, Dormans JP, Weiss AR. Randomized controlled trial of interval-compressed chemotherapy for the treatment of localized Ewing sarcoma: a report from the Children's Oncology Group. J Clin Oncol. 2012 Nov 20;30(33):4148-54. doi: 10.1200/JCO.2011.41.5703. Epub 2012 Oct 22. Erratum In: J Clin Oncol. 2015 Mar 1;33(7):814. doi: 10.1200/JCO.2015.61.1491.. Dosage error in article text. PubMed 23091096 ↗
  • Borinstein SC, Barkauskas DA, Krailo M, Scher D, Scher L, Schlottmann S, Kallakury B, Dickman PS, Pawel BR, West DC, Womer RB, Toretsky JA. Investigation of the insulin-like growth factor-1 signaling pathway in localized Ewing sarcoma: a report from the Children's Oncology Group. Cancer. 2011 Nov 1;117(21):4966-76. doi: 10.1002/cncr.26112. Epub 2011 Apr 8. PubMed 21480204 ↗
  • Womer RB, West DC, Krailo MD, et al.: Randomized comparison of every-two-week v. every-three-week chemotherapy in Ewing sarcoma family tumors (ESFT). [Abstract] J Clin Oncol 26 (Suppl 15): A-10504, 2008.
  • Mora J, Castaneda A, Perez-Jaume S, Lopez-Pousa A, Maradiegue E, Valverde C, Martin-Broto J, Garcia Del Muro X, Cruz O, Cruz J, Martinez-Trufero J, Maurel J, Vaz MA, de Alava E, de Torres C. GEIS-21: a multicentric phase II study of intensive chemotherapy including gemcitabine and docetaxel for the treatment of Ewing sarcoma of children and adults: a report from the Spanish sarcoma group (GEIS). Br J Cancer. 2017 Sep 5;117(6):767-774. doi: 10.1038/bjc.2017.252. Epub 2017 Aug 8. PubMed 28787430 ↗
09

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of May 2001, a primary completion of Aug 2006 and a completion of Jun 2023. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Dec 6, 2000
First posted
Jan 27, 2003
Start
May 2001
Primary completionActual
Aug 2006
CompletionActual
Jun 30, 2023
Last update
Aug 3, 2023
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 3, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00006734
Responsible party
Sponsor
First posted
Jan 27, 2003
Start date
May 2001
Primary completion
Aug 2006
Completion
Jun 30, 2023
Last update
Aug 3, 2023

Study contacts

Richard B. Womer, MD
study chair · Children's Hospital of Philadelphia

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Aug 2023. You cannot join it, but the record below documents what was studied.

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Discussion

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Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Studies of the drugs tested here: Filgrastim · Cyclophosphamide · Doxorubicin · Etoposide · Ifosfamide · Vincristine

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